Evidence map›Paper›PMID 34532786›Full record

ReviewMolecular neurobiology2021

Application of Metabolomics to the Discovery of Biomarkers for Ischemic Stroke in the Murine Model: a Comparison with the Clinical Results.

Jinjing Jia, Hangyao Zhang, Xiaoyi Liang, Yuning Dai, Lihe Liu, Kaiwen Tan, Ruohan Ma, Jiahuan Luo, Yi Ding, Chaofu Ke

Erratum issuedAbstract readReview
PubMed Publisher
In one paragraph

Review in Molecular neurobiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 29 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 2 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

29 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Frontiers in pharmacology · 2024
    Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Jinjing JiaMedical College of Soochow University, 199 Renai Road, Suzhou, 215123, People's Republic of China.
Hangyao ZhangMedical College of Soochow University, 199 Renai Road, Suzhou, 215123, People's Republic of China.
Xiaoyi LiangMedical College of Soochow University, 199 Renai Road, Suzhou, 215123, People's Republic of China.
Yuning DaiMedical College of Soochow University, 199 Renai Road, Suzhou, 215123, People's Republic of China.
Lihe LiuMedical College of Soochow University, 199 Renai Road, Suzhou, 215123, People's Republic of China.
Kaiwen TanMedical College of Soochow University, 199 Renai Road, Suzhou, 215123, People's Republic of China.
Ruohan MaMedical College of Soochow University, 199 Renai Road, Suzhou, 215123, People's Republic of China.
Jiahuan LuoMedical College of Soochow University, 199 Renai Road, Suzhou, 215123, People's Republic of China.
Yi DingDepartment of Preventive Medicine, College of Clinical Medicine, Suzhou Vocational Health College, Suzhou, 215009, People's Republic of China.
Chaofu KeDepartment of Epidemiology and Biostatistics, School of Public Health, Medical College of Soochow University, 199 Renai Road, Suzhou, 215123, People's Republic of China. cfke@suda.edu.cn.ORCID http://orcid.org/0000-0003-3188-4307

Funding

National Natural Science Foundation of China 81703316
6 · The paper itself

Abstract

Ischemic stroke (IS) is a major cause of mortality and disability worldwide. However, the pathogenesis of IS remains unknown, and methods for early prediction and diagnosis of IS are lacking. Metabolomics can be applied to biomarker discovery and mechanism exploration of IS by exploring metabolic alterations. In this review, 62 IS metabolomics studies in the murine model published from January 2006 to December 2020 in the PubMed and Web of Science databases were systematically reviewed. Twenty metabolites (e.g., lysine, phenylalanine, methionine, tryptophan, leucine, lactate, serine, N-acetyl-aspartic acid, and glutathione) were reported consistently in more than two-third murine studies. The disturbance of metabolic pathways, such as arginine biosynthesis; alanine, aspartate and glutamate metabolism; aminoacyl-tRNA biosynthesis; and citrate cycle, may be implicated in the development of IS by influencing the biological processes such as energy failure, oxidative stress, apoptosis, and glutamate toxicity. The transient middle cerebral artery occlusion model and permanent middle cerebral artery occlusion model exhibit both common and distinct metabolic patterns. Furthermore, five metabolites (proline, serine, LysoPC (16:0), uric acid, glutamate) in the blood sample and 7 metabolic pathways (e.g., alanine, aspartate, and glutamate metabolism) are shared in animal and clinical studies. The potential biomarkers and related pathways of IS in the murine model may facilitate the biomarker discovery for early diagnosis of IS and the development of novel therapeutic targets.

Indexed as

MetabolomicsAnimalsBiomarkersDisease Models, AnimalHumansIschemic StrokeMiceBiomarkersBiomarkerIschemic strokeMetabolic pathwayMetabolomicsMurine model

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.